Background <p>Breast phyllodes tumors (PT) are classified as benign, borderline, or malignant, primarily based on histological features, but lack reliable biomarkers for grading. Our aim is to find a protein marker to improve the accuracy of PT grading.</p> Methods <p>We analyzed formalin-fixed paraffin-embedded (FFPE) samples of fibroadenoma (FA) and PT using quantitative proteomics to screen the protein marker S100A8, confirmed its role in PT grading via immunohistochemistry, and examined its correlation with clinicopathological features.</p> Results <p>Quantitative proteomics studies showed that the differential proteins between FA and PT primarily involve calcium ion binding, including S100A8, FKBP10, MMP9, SPARC, and MMP14. Meanwhile, the proteomic studies showed a statistically significant increase in the expression of S100A8 in malignant PT compared with benign PT. Immunohistochemical validation showed that S100A8 was predominantly expressed in the nucleus and cytoplasm of stromal cells in malignant PT. The expression level of S100A8 in stromal cells demonstrated a positive correlation with PT categories (<i>p</i>&#xa0;&lt;&#xa0;.001), as well as with Ki67 expression (<i>p</i>&#xa0;&lt;&#xa0;.001).</p> Conclusions <p>To the best of our knowledge, this study is the first to demonstrate the integration of S100A8 and Ki67 expression in stromal cells with histological characteristics aids in grading PT.</p>

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From Proteomics to Pathology: S100A8’s Impact on Breast Phyllodes Tumors Grading

  • Yan Shao,
  • Xiaoyang Wang,
  • Jiali Yang,
  • Yi Huang,
  • Lili Qian,
  • Yu Xie,
  • Meihua Ye,
  • Juan Liu,
  • Yanling Jin

摘要

Background

Breast phyllodes tumors (PT) are classified as benign, borderline, or malignant, primarily based on histological features, but lack reliable biomarkers for grading. Our aim is to find a protein marker to improve the accuracy of PT grading.

Methods

We analyzed formalin-fixed paraffin-embedded (FFPE) samples of fibroadenoma (FA) and PT using quantitative proteomics to screen the protein marker S100A8, confirmed its role in PT grading via immunohistochemistry, and examined its correlation with clinicopathological features.

Results

Quantitative proteomics studies showed that the differential proteins between FA and PT primarily involve calcium ion binding, including S100A8, FKBP10, MMP9, SPARC, and MMP14. Meanwhile, the proteomic studies showed a statistically significant increase in the expression of S100A8 in malignant PT compared with benign PT. Immunohistochemical validation showed that S100A8 was predominantly expressed in the nucleus and cytoplasm of stromal cells in malignant PT. The expression level of S100A8 in stromal cells demonstrated a positive correlation with PT categories (p < .001), as well as with Ki67 expression (p < .001).

Conclusions

To the best of our knowledge, this study is the first to demonstrate the integration of S100A8 and Ki67 expression in stromal cells with histological characteristics aids in grading PT.